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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 274171Erstellt: 25. Oktober 2026

Acetic Acid → 1-Phenyl-3-acetoxybutane

https://huagongshe.com/reaction/274171

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktHydrochloric AcidHCID 313—
EduktTolueneHCID 1140—
Edukt4-Phenyl-2-butanolHCID 61302—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelPyridineHCID 1049—
Produkt1-Phenyl-3-acetoxybutaneHCID 6151798,5%

Reaktionsschritte

Into a four-necked flask provided with a thermometer and a stirrer, 150 g (1 mol) of 4-phenyl-2-butanol (XXX-35), 500 ml of toluene and 200 ml of pyridine were charged. 122.4 g (1.2 mol) of anhydrous acetic acid and 1 g of 4-dimethylaminopyridine were further added thereto to react them for 4 hours, while temperature being maintained at 40°-50° C. After completion of the reaction, the reaction mixture was poured into 500 ml of 4N hydrochloric acid solution, extracted and fractionated, and then an organic layer was washed with 1N hydrochloric acid, water, 5% sodium bicarbonate solution and water in the order. The thus-obtained Organic layer was concentrated under a reduced pressure to obtain 189 g of 2-acetoxy-4-phenylbutane (XXIX-35) with yield of 98.5%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05389293
Quelldatensatzuspto-grants-1995_02
ORD IDord-4a027c600c1b409fa64f0e264bc8a4d8
Quellennotizuspto-grants-1995_02